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Application of outpatient cardiac testing among emergency department patients with syncope

机译:急诊心脏试验在急诊部患者晕厥患者中的应用

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2.6% of ED syncope patients will suffer cardiac serious adverse events (SAEs) within 30?days of disposition, and outpatient cardiac testing can improve patient safety. The objective is to determine whether outpatient cardiac testing for ED syncope patients is being appropriately ordered after discharge. To this end, we describe the proportion of high-risk and non-high (low and medium)-risk ED syncope patients as per the Canadian Syncope Risk Score (CSRS) who have a SAE after ED discharge, and the proportion referred for outpatient cardiac testing.Our multicentre prospective cohort study enrolled adult syncope patients between 2010 and 2014 in five academic EDs. We collected patient characteristics, disposition, CSRS predictors, outpatient referrals and testing results (Holter, echocardiography), and 30-day adjudicated SAE (death due to unknown/cardiac cause, myocardial infarction, arrhythmia and structural heart disease). We used descriptive statistics (mean, SD) to report our results.Of 3584 enrolled patients (mean age 50.9 years, 57.7% women), 800 patients (22.3%) received an outpatient referral. Of these 800 patients, 40.3% of the non-high-risk patients (305/756) and 54.5% of the high-risk patients (24/44) received outpatient cardiac testing. Of all patients who received cardiac testing, five (1.5%; 95%?CI 0.6% to 3.5%) suffered outpatient SAE (60.0% arrhythmias). Of all patients who did not receive cardiac testing, four patients (0.9%; 95%?CI 0.3% to 2.2%) suffered SAE (all arrhythmias). Of the 20 (45.5%) high-risk patients who did not receive testing, two patients (10.0%; 95%?CI 2.8% to 30.1%) suffered arrhythmias outside the hospital, while among the 451 (59.7%) non-high-risk patients, only two (0.4%; 95%?CI 0.1% to 1.6%) suffered outpatient arrhythmias.Outpatient cardiac testing is largely underused, especially among high-risk ED syncope patients. Better guidelines for outpatient cardiac testing are needed, as the practice is highly variable and mismatched with patient risk.
机译:2.6%的ED Syncope患者将在30?日内患有心脏严重不良事件(SAES),并且门诊心脏测试可以提高患者安全性。目的是确定ED Syncope患者的门诊心脏测试是否在放电后适当地订购。为此,我们描述高风险和非高(低和中等)-RISK ED晕厥患者的比例,根据加拿大晕厥的风险评分(CSR),在ED放电后具有SAE,以及外部的比例心脏测试。我们多中心前瞻性队列研究在2010年至2014年期间参加了成人晕厥患者在五个学术署。我们收集了患者特征,处置,CSRS预测因子,门诊引导和测试结果(HOLTER,超声心动图)和30天判决的SAE(由于未知/心脏病,心肌梗塞,心律失常和结构心脏病)。我们使用描述性统计(平均值,SD)报告我们的结果。3584名患者(平均年龄为50.9岁,57.7%的妇女),800名患者(22.3%)接受了门诊转诊。在这800名患者中,40.3%的非高风险患者(305/756)和54.5%的高风险患者(24/44)接受了门诊心脏测试。所有接受心脏检测的患者中,五个(1.5%; 95%?CI 0.6%至3.5%)遭受了门诊SAE(60.0%心律失常)。所有没有接受心脏病测试的患者,4名患者(0.9%; 95%?CI 0.3%至2.2%)遭受SAE(所有心律失常)。 20(45.5%)未接受测试的高风险患者,两名患者(10.0%; 95%?CI 2.8%至30.1%)在医院外遭受心律失常,而451(59.7%)非高高-RISK患者,只有两次(0.4%; 95%?CI 0.1%至1.6%)遭受门诊心律失常。诱惑心脏测试在很大程度上未被发救,特别是在高风险的ED晕厥患者中。需要更好的门诊心脏测试准则,因为这种做法具有高度变量和患者风险不匹配。

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